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Details
Link-It Detail - Disease - 6-32 DISORDERS OF COPPER METABOLISM
Debug Stats
  • ### Total Build Time: 137 ms 13.596 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=7 ms Completed: 7 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=67 ms Completed: 67 ms rowSize= 7.304 KB
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 4.693 KB
  • CONCEPT_XREFS gt=34 ms Completed: 34 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
6-32 DISORDERS OF COPPER METABOLISM C0012714
Relationships (16)

Relation Types:
diso_​to_​chem : 1
diso_​to_​diso : 14
diso_​to_​phys : 1


Relationships:
associated_​with : 3
classifies : 2
isa : 6
mapped_​to : 5
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEMassociated_withimg Copper C0009968
DISO_to_DISOclassifiesimg 6-30 DISORDERS OF MINERAL METABOLISM: GENERAL TERMS C0154260
DISO_to_DISOmapped_toimg 6-32 DISORDERS OF COPPER METABOLISM C0012714
DISO_to_DISOmapped_toimg Chronic copper deficiency C0268070
DISO_to_DISOisaimg Cutis laxa, x-linked C0268353
DISO_to_DISOassociated_withimg Disease C0012634
DISO_to_DISOmapped_toimg Familial hypoceruloplasminaemia C0268073
DISO_to_DISOmapped_toimg Hepatolenticular Degeneration C0019202
DISO_to_DISOisaimg Hypercupraemia C0268072
DISO_to_DISOisaimg Hypercupruria C1263723
DISO_to_DISOisaimg Indian childhood cirrhosis C0268074
DISO_to_DISOmapped_toimg Menkes Kinky Hair Syndrome C0022716
DISO_to_DISOisaimg Nutritional myelopathy of pigs C0268071
DISO_to_DISOclassifiesimg Other endo metab nutri disease C0497409
DISO_to_DISOisaimg Swayback C0038981
DISO_to_PHYSassociated_withimg Metabolism C0025519
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD1150684copper metabolism (Murr1) domain containing 1
img GENERIF, Score=913, Pubmed Id: 16283886, UMLKSK CUI: C0012714
HumanPRNP5621prion protein
img GENERIF, Score=686, Pubmed Id: 16831968, UMLKSK CUI: C0012714
HumanATP7B540ATPase, Cu++ transporting, beta polypeptide
img GENERIF, Score=913, Pubmed Id: 14616767, UMLKSK CUI: C0012714
HumanXIAP331X-linked inhibitor of apoptosis
img GENERIF, Score=913, Pubmed Id: 16543147, UMLKSK CUI: C0012714
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C00127146-32 DISORDERS OF COPPER METABOLISM0self